10,000 publications from this institution
We ask whether epidemic exposure leads to a shift in financial technology usage within and across countries and if so who participates in this shift. We exploit a datasetcombining Gallup World Polls and Global Findex surveys for some 250,000 individuals in 140 countries, merging them with information on the incidence of epidemics and local 3G internet infrastructure. Epidemic exposure is associated with an increase in remote-access (online/mobile) banking and substitution from bank branch-based to ATM-based activity. Using a machine-learning algorithm, we show that heterogeneity in this response centers on the age, income and employment of respondents. Young, high-income earners in full-time employment have the greatest propensity to shift to online/mobile transactions in response to epidemics. These effects are larger for individuals in subnational regions with better ex ante 3G signal coverage, highlighting the role of the digital divide in adaption to new technologies necessitated by adverse external shocks.
Abstract The asymmetric fluorination of substituted cyclohexanones generates quaternary fluorine‐containing stereocenters through the combination of two separate catalytic cycles: enamine activation of the ketone and chiral anion phase‐transfer activation of the fluorination agent.
A new molecular precursor strategy has been used to prepare a series of single-site catalysts that possess isolated iron centers supported on mesoporous SBA-15 silica. The iron centers were introduced via grafting reactions of the tris(tert-butoxy)siloxy iron(III) complex Fe[OSi(O(t)Bu)(3)](3)(THF) with SBA-15 in dry hexane. This complex reacts cleanly with the hydroxyl groups of SBA-15 to eliminate HOSi(O(t)Bu)(3) (as monitored by (1)H NMR spectroscopy) with formation of isolated surface species of the type identical with SiO-Fe-[OSi(O(t)Bu)(3)](2)(THF). In this way, up to 21% of the hydroxyl sites on SBA-15 were derivatized (0.23 Fe nm(-)(2)), and iron loadings in the range of 0.0-1.90% were achieved. The structure of the surface-bound iron species, as determined by spectroscopic methods (electron paramagnetic resonance (EPR), nuclear magnetic resonance (NMR), UV-vis, and in situ infrared measurements) and by elemental analyses, contains a pseudotetrahedral iron(III) center. The THF ligand of this surface-bound complex was quantitatively displaced by acetonitrile (by (1)H NMR spectroscopy). Calcination of these materials at 300 degrees C for 2 h under oxygen resulted in removal of all organic matter and site-isolated iron surface species that are stable to condensation to iron oxide clusters. Spectroscopic data (UV-vis and EPR) suggest that the iron centers retain a mononuclear, pseudotetrahedral iron(III) structure after calcination. The calcinated, iron-grafted SBA-15 materials exhibit high selectivities as catalysts for oxidations of alkanes, alkenes, and arenes, with hydrogen peroxide as the oxidant.
We have discovered that a class of inorganic sulfides [Li2S, (NH4)2S, Na2S⋅9H2O, etc.] imparts excellent electronic properties to GaAs surfaces. The surface recombination velocity at the interface between Na2S⋅9H2O and GaAs begins to approach that of the nearly ideal AlGaAs/GaAs interface. We propose the formation of a robust covalently bonded sulfide layer to explain the favorable electronic quality of such interfaces.
Multivalent batteries offer potential advantages over lithium-ion batteries but face challenges due to limited ionic mobility in solid-state cathodes. Recent investigations have demonstrated that incorporating multivalent cations, particularly calcium ions (Ca 2+ ), into monovalent cathodes such as NaSICON and R-3m NaV 2 (PO 4 ) 3 , results in improved capacity retention. This study investigates the phase evolution and charging mechanism in these dual cation cathodes by using a cluster expansion and charge-neutral Monte Carlo simulation in a Ca-Na-V 2 (PO 4 ) 3 system. Our results found that during the discharge with either Ca or Na ions, phase transitions occurs when the oxidation state of the transition metal changes, in particular between Na 1 V 2 (PO 4 ) 3 - Na 3 V 2 (PO 4 ) 3 and Na 1 V 2 (PO 4 ) 3 - Ca 1 V 2 (PO 4 ) 3 . This behavior suggests that the charging pathway of Na/Ca ions can be altered by varying the Ca/Na chemical potential. Figure 1
Este artículo analiza el enfoque del autor sobre la etnografía, la teoría social, y la política del conocimiento a través de un diálogo que vuelve sobre su trayectoria intelectual y los vínculos analíticos entre sus investigaciones sobre el cuerpo, la marginalidad urbana comparada y el Estado penal. Resalta las conexiones prácticas y fundamentos epistemológicos detrás de sus principales proyectos de investigación, explica las distintas maneras en que se despliega el trabajo de campo de observación en cada uno de ellos, y examina el papel de los intelectuales en las sociedades avanzadas de la era del neoliberalismo hegemónico. Rechazando tanto el empirismo de Hume como el neo-cognitivismo kantiano, el autor aboga por el uso de la etnografía como un instrumento de ruptura y construcción, la potencia del conocimiento carnal, el imperativo de la reflexividad epistémica y la necesidad de ampliar los géneros textuales y estilos con el fin de captar mejor el sabor y el dolor de la acción social. En la esfera pública, propone que las ciencias sociales pueden actuar como un disolvente de la doxa y un faro que arroja luz sobre las propiedades latentes y las tendencias desapercibidas en las transformaciones sociales a fin de generar rupturas y ampliar el debate cívico.
This book is mainly based on the first and second symposia on Nanotechnology in Catalysis held in 2001 and 2002, but it also includes several contributions not presented in the symposia to round out the scope of the subject. The contents are the most up to date developments made by researchers all over the world in the catalysis field in this fascinating nanotechnology era. It reflects some of the frontier areas of nanoscience and nanotechnology in fabricating and characterizing catalysts and carrying out studies to prove their superior selectivity and activity. The field of application of nanotechnology for the development of catalysts for green chemistry is likely to grow rapidly during the next decade. This book hopes to contribute to the evolution of nanotechnology in that direction.